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NOT YET RECRUITING
NCT07655804
PHASE3

Subcutaneous Calcitonin in Acute Herpes Zoster

Sponsor: Tanta University

View on ClinicalTrials.gov

Summary

This prospective randomized controlled study will be conducted to evaluate the effect of adding calcitonin to the standard treatment protocol in patients with acute herpes zoster infection.

Official title: The Prophylactic Value of Subcutaneous Calcitonin in Acute Herpes Zoster Patients: A Randomized Controlled Trial

Key Details

Gender

All

Age Range

50 Years - Any

Study Type

INTERVENTIONAL

Enrollment

168

Start Date

2026-07-01

Completion Date

2027-10-01

Last Updated

2026-06-18

Healthy Volunteers

No

Interventions

DRUG

Calcitonin

patients will receive subcutaneous salmon calcitonin 100 IU (ampoule = 1 ml) daily for three weeks

OTHER

Saline

patients will receive subcutaneous saline (1 ml) daily for three weeks.

Locations (1)

Tanta University Hospitals

Tanta, Gharbia Governorate, Egypt